材料科学
异质结
阳极
氧化物
兴奋剂
化学工程
电化学动力学
纳米颗粒
电极
硫化物
动力学
离子
纳米技术
电化学
光电子学
物理化学
量子力学
物理
工程类
化学
冶金
作者
Can Guo,Wenchao Zhang,Yi Liu,Jiapeng He,Shun Yang,Mingkai Liu,Qinghong Wang,Zhanhu Guo
标识
DOI:10.1002/adfm.201901925
摘要
Abstract Heterostructures are attractive for advanced energy storage devices due to their rapid charge transfer kinetics, which is of benefit to the rate performance. The rational and facile construction of heterostructures with satisfactory electrochemical performance, however, is still a great challenge. Herein, ultrafine hetero‐CoO/Co 3 S 4 nanoparticles embedded in N‐doped carbon frameworks (CoO/Co 3 S 4 @N‐C) are successfully obtained by employing metal‐organic frameworks as precursors. As anodes for sodium ion batteries, the CoO/Co 3 S 4 @N‐C electrodes exhibit high specific capacity (1029.5 mA h g −1 at 100 mA g −1 ) and excellent rate capability (428.0 mA h g −1 at 5 A g −1 ), which may be attributed to their enhanced electric conductivity, facilitated Na + transport, and intrinsic structural stability. Density functional theoretical calculations further confirm that the constructed heterostructures induce electric fields and promote fast reaction kinetics in Na + transport. This work provides a feasible approach to construct metal oxide/sulfide heterostructures toward high‐performance metal‐ion batteries.
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